Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

21.3 INCH(54 CM) MONOCHROME LCD MONITOR MS25I2(ML21025)

K-Number: K133511 · 2013-12-19

ApplicantJvckenwood Corporation
Decision Date2013-12-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

21.3 INCH(54 CM) MONOCHROME LCD MONITOR MS25I2(ML21025) is the device name listed in this FDA 510(k) record. The listed applicant is Jvckenwood Corporation. It received FDA 510(k) clearance on 2013-12-19 under 510(k) number K133511. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 21.3 INCH(54 CM) MONOCHROME LCD MONITOR MS25I2(ML21025)?

21.3 INCH(54 CM) MONOCHROME LCD MONITOR MS25I2(ML21025) is a medical device that received FDA 510(k) clearance on 2013-12-19. The listed applicant is Jvckenwood Corporation. The 510(k) number is K133511.

When did 21.3 INCH(54 CM) MONOCHROME LCD MONITOR MS25I2(ML21025) receive FDA 510(k) clearance?

21.3 INCH(54 CM) MONOCHROME LCD MONITOR MS25I2(ML21025) received FDA 510(k) clearance on 2013-12-19, under 510(k) number K133511.

Who is the listed applicant for 21.3 INCH(54 CM) MONOCHROME LCD MONITOR MS25I2(ML21025)?

The FDA 510(k) record lists Jvckenwood Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 21.3 INCH(54 CM) MONOCHROME LCD MONITOR MS25I2(ML21025)?

The FDA product code for 21.3 INCH(54 CM) MONOCHROME LCD MONITOR MS25I2(ML21025) is LLZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Jvckenwood Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K2411053MP Color LCD Monitor (CL-S301)K2228648MP Color LCD Monitor CL-R813K2129856MP Color LCD Monitor CL-S600K20373312MP Color Digital Mammography LCD Monitor CL-S1200K2103452MP Monochrome LCD Monitor MS-S200K2001613MP Monochrome Digital Mammography LCD Monitor MS-S300

View all 15 devices →

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑